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Danaher Corporation Quality Control Supervisor - 12 hour nights in Newark, California

At Cepheid, we are passionate about improving health care through faster, more accurate diagnostic tests. As a member of our team, you’ll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission drives us, every moment of every day, as we develop rapid groundbreaking solutions to solve the world’s most complex health challenges.

Our associates are involved in every stage of molecular diagnostics ­ ­­– from ideation and innovation through development and delivery of life-changing advancements in healthcare-associated infections, sexual health, critical infectious disease, virology and oncology applications. For more details, visit us at www.cepheid.com or follow us on Twitter. (@CepheidNews)

As part of the Danaher family of companies, our work at Cepheid is supported by a global science and technology innovator. In addition to Danaher’s unrivaled leadership training and professional development programs, this relationship also provides expanded career opportunities across industries and brands. Together, we are united by a shared purpose: Helping Realize Life’s Potential.

This is a night shift position.

6:00pm to 6:00am. F lexibility needed for the following weekly rotation:

Week 1 Sunday, Monday and Tuesday

Week 2 Sunday, Monday, Tuesday and Wednesday

This Quality Control Supervisor works to that operations at Cepheid meet client requirements and cGMP regulations via Quality Control staff. The QC Supervisor will ensure responsiveness to clients and overall client satisfaction. The successful individual is responsible for coordinating and implementing activities to attain strategic objectives within the department and looks to his or her direct supervisor or other peers within the industry for guidance. In addition, the QC Supervisor is able to establish goals and objectives, supervise work practices for their direct reports, will interpret and execute policies and procedures that typically affect organizational units. This position will interact with other departments and/or divisions within Cepheid.

ESSENTIAL JOB RESPONSIBILITIES:

  • Manages the Quality Control department daily work activities including: Team schedule, ensuring training, general guidance to direct reports and across functional groups, and serves as resource for technical / administrative problems.

  • Hires, trains, motivates, leads, develops and evaluates staff. Takes corrective action as necessary on a timely basis and in accordance with company policy.

  • Ensures Quality Control systems are compliant with corporate and site procedures, as well as industry standards.

  • Supports development of novel QC analytical methods. Works in conjunction with other departments to develop, qualify, and transfer QC analytical methods as applicable.

  • Ensures maintenance of QC equipment – qualification, calibration and maintenance.

  • Drafts, reviews, and approves Standard Operating Procedures (SOP), sampling plans, specifications, protocols and reports related to product/processes, equipment, method, validation. This includes deviation investigation and reporting.

  • Develops and implements statistical tools for Quality Systems monitoring and review.

  • Identifies and implements improvement opportunities for established Quality Systems, processes, procedures, and training to support CAPA, Change Control, Deviation, Risk Management, and Investigation processes.

  • Lead investigations for failures during Quality control testing; perform troubleshooting, process development or improvement activities.

TRAINING RESPONSIBILITIES:

  • Complete all assigned and required training satisfactorily and on time

  • For people managers, ensure your associates attend and complete all required trainings satisfactorily and on time.

MINIMUM REQUIREMENTS:

Education or Experience:

  • High school degree with 8+ years of experience or Bachelor’s degree with 5+ years of experience OR Master’s degree with 3+ years of experience

  • Experience with managing people and providing leadership.

  • Thorough knowledge of cGMP regulations related to Quality Control required.

Knowledge and skills:

  • Experience with analytical method, and Microbiology testing.

  • Proven track record in method validation / qualification and qualification of equipment / systems.

  • Experience with facility / laboratory expansions.

  • Experience in a QC support in high pace manufacturing setting.

When you join us, you’ll also be joining Danaher’s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) tools and the stability of a tested organization.Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.The EEO posters are available here (https://www.dol.gov/agencies/ofccp/posters) .We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at 202.419.7762 or applyassistance@danaher.com to request accommodation.If you’ve ever wondered what’s within you, there’s no better time to find out.

Operating Company: Cepheid

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